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Variants search result for Homo sapiens
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75 records found for search term Galnt6
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15147067CV779534single nucleotide variantNM_007210.4(GALNT6):c.1755+7C>Tnot provided [RCV000967267]benign125135579951355799Humanname
598203341CV3973937single nucleotide variantNM_007210.4(GALNT6):c.27G>A (p.Met9Ile)not specified [RCV005337242]uncertain significance125137975551379755Humanname
407503577CV3436324single nucleotide variantNM_007210.4(GALNT6):c.65T>C (p.Leu22Pro)not specified [RCV004623797]uncertain significance125137971751379717Humanname
15139397CV713570single nucleotide variantNM_007210.4(GALNT6):c.543G>A (p.Val181=)not provided [RCV000965960]benign125137731651377316Humanname
156080981CV2255994single nucleotide variantNM_007210.4(GALNT6):c.239A>G (p.Gln80Arg)not specified [RCV004122438]uncertain significance125137954351379543Humanname
156071240CV2267222single nucleotide variantNM_007210.4(GALNT6):c.149A>G (p.Lys50Arg)not specified [RCV004133904]uncertain significance125137963351379633Humanname
156005648CV2281612single nucleotide variantNM_007210.4(GALNT6):c.125G>C (p.Trp42Ser)not specified [RCV004153907]uncertain significance125137965751379657Humanname
156152993CV2377666single nucleotide variantNM_007210.4(GALNT6):c.202A>G (p.Met68Val)not specified [RCV004227842]uncertain significance125137958051379580Humanname
401727861CV2678526single nucleotide variantNM_007210.4(GALNT6):c.131A>G (p.Lys44Arg)not specified [RCV004292538]uncertain significance125137965151379651Humanname
401749763CV2719392single nucleotide variantNM_007210.4(GALNT6):c.271C>T (p.Pro91Ser)not specified [RCV004325015]uncertain significance125137951151379511Humanname
401876658CV2767668single nucleotide variantNM_007210.4(GALNT6):c.146G>A (p.Arg49Gln)not specified [RCV004345805]likely benign125137963651379636Humanname
401932135CV2807004single nucleotide variantNM_007210.4(GALNT6):c.1704C>T (p.Phe568=)not provided [RCV003391821]likely benign125135585751355857Humanname
407503560CV3436319single nucleotide variantNM_007210.4(GALNT6):c.145C>T (p.Arg49Trp)not specified [RCV004623792]uncertain significance125137963751379637Humanname
597754067CV3680726single nucleotide variantNM_007210.4(GALNT6):c.103G>A (p.Glu35Lys)not specified [RCV004924285]uncertain significance125137967951379679Humanname
597779970CV3680728single nucleotide variantNM_007210.4(GALNT6):c.204G>A (p.Met68Ile)not specified [RCV004930510]uncertain significance125137957851379578Humanname
597779996CV3680737single nucleotide variantNM_007210.4(GALNT6):c.106G>A (p.Glu36Lys)not specified [RCV004930516]uncertain significance125137967651379676Humanname
598203328CV3973935single nucleotide variantNM_007210.4(GALNT6):c.137T>C (p.Leu46Pro)not specified [RCV005337240]uncertain significance125137964551379645Humanname
155945221CV2237954single nucleotide variantNM_007210.4(GALNT6):c.512G>A (p.Arg171Gln)not specified [RCV004110995]uncertain significance125137734751377347Humanname
156166387CV2270413single nucleotide variantNM_007210.4(GALNT6):c.917T>C (p.Phe306Ser)not specified [RCV004137390]uncertain significance125136425351364253Humanname
156171995CV2312614single nucleotide variantNM_007210.4(GALNT6):c.561C>G (p.Asn187Lys)not specified [RCV004169352]uncertain significance125137729851377298Humanname
156187070CV2324776single nucleotide variantNM_007210.4(GALNT6):c.431C>T (p.Ala144Val)not specified [RCV004173010]uncertain significance125137935151379351Humanname
156173901CV2326891single nucleotide variantNM_007210.4(GALNT6):c.886C>A (p.Pro296Thr)not specified [RCV004176713]uncertain significance125136428451364284Humanname
156169462CV2345557single nucleotide variantNM_007210.4(GALNT6):c.773G>C (p.Ser258Thr)not specified [RCV004198314]uncertain significance125136547151365471Humanname
156208932CV2382568single nucleotide variantNM_007210.4(GALNT6):c.524C>T (p.Pro175Leu)not specified [RCV004232896]uncertain significance125137733551377335Humanname
155998448CV2393425single nucleotide variantNM_007210.4(GALNT6):c.524C>G (p.Pro175Arg)not specified [RCV004228922]uncertain significance125137733551377335Humanname
329385018CV2435235single nucleotide variantNM_007210.4(GALNT6):c.332A>G (p.Asn111Ser)not specified [RCV004252871]uncertain significance125137945051379450Humanname
401761511CV2702370single nucleotide variantNM_007210.4(GALNT6):c.721G>A (p.Val241Met)not specified [RCV004316897]uncertain significance125136552351365523Humanname
401736066CV2703034single nucleotide variantNM_007210.4(GALNT6):c.864G>C (p.Glu288Asp)not specified [RCV004321340]uncertain significance125136430651364306Humanname
401872363CV2754348single nucleotide variantNM_007210.4(GALNT6):c.611C>T (p.Thr204Ile)not specified [RCV004334524]uncertain significance125137724851377248Humanname
405750101CV3254527single nucleotide variantNM_007210.4(GALNT6):c.409T>C (p.Tyr137His)not specified [RCV004392607]uncertain significance125137937351379373Humanname
405750108CV3254528single nucleotide variantNM_007210.4(GALNT6):c.416A>G (p.Lys139Arg)not specified [RCV004392608]uncertain significance125137936651379366Humanname
405750114CV3254529single nucleotide variantNM_007210.4(GALNT6):c.562G>A (p.Glu188Lys)not specified [RCV004392609]uncertain significance125137729751377297Humanname
405750119CV3254530single nucleotide variantNM_007210.4(GALNT6):c.757C>T (p.Arg253Trp)not specified [RCV004392610]uncertain significance125136548751365487Humanname
405750127CV3254531single nucleotide variantNM_007210.4(GALNT6):c.895G>C (p.Val299Leu)not specified [RCV004392611]uncertain significance125136427551364275Humanname
407503548CV3436316single nucleotide variantNM_007210.4(GALNT6):c.545T>A (p.Ile182Asn)not specified [RCV004623789]uncertain significance125137731451377314Humanname
407503564CV3436320single nucleotide variantNM_007210.4(GALNT6):c.901A>T (p.Ile301Phe)not specified [RCV004623793]uncertain significance125136426951364269Humanname
407503567CV3436321single nucleotide variantNM_007210.4(GALNT6):c.619A>C (p.Ile207Leu)not specified [RCV004623794]uncertain significance125137724051377240Humanname
407503570CV3436322single nucleotide variantNM_007210.4(GALNT6):c.748A>C (p.Ile250Leu)not specified [RCV004623795]uncertain significance125136549651365496Humanname
597754071CV3680729single nucleotide variantNM_007210.4(GALNT6):c.467T>C (p.Leu156Pro)not specified [RCV004924286]uncertain significance125137931551379315Humanname
597779980CV3680732single nucleotide variantNM_007210.4(GALNT6):c.961G>A (p.Gly321Ser)not specified [RCV004930512]uncertain significance125136420951364209Humanname
597779984CV3680734single nucleotide variantNM_007210.4(GALNT6):c.865G>C (p.Asp289His)not specified [RCV004930513]uncertain significance125136430551364305Humanname
598203335CV3973936single nucleotide variantNM_007210.4(GALNT6):c.969T>G (p.Phe323Leu)not specified [RCV005337241]uncertain significance125136420151364201Humanname
598158872CV3973940single nucleotide variantNM_007210.4(GALNT6):c.725G>A (p.Arg242Gln)not specified [RCV005328151]uncertain significance125136551951365519Humanname
15135142CV713571single nucleotide variantNM_007210.4(GALNT6):c.414G>C (p.Lys138Asn)not provided [RCV000965239]benign125137936851379368Humanname
8634712CV89932single nucleotide variantNM_007210.3(GALNT6):c.302C>T (p.Pro101Leu)Malignant melanoma [RCV000070029]not provided125137948051379480Humanname
156263542CV2201174single nucleotide variantNM_007210.4(GALNT6):c.1426A>G (p.Asn476Asp)not specified [RCV004077323]uncertain significance125135820451358204Humanname
156031550CV2239162single nucleotide variantNM_007210.4(GALNT6):c.1439A>G (p.Tyr480Cys)not specified [RCV004112150]uncertain significance125135819151358191Humanname
156173604CV2247612single nucleotide variantNM_007210.4(GALNT6):c.1281T>A (p.Asn427Lys)not specified [RCV004108904]uncertain significance125135921951359219Humanname
156155994CV2266181single nucleotide variantNM_007210.4(GALNT6):c.1526G>T (p.Cys509Phe)not specified [RCV004128760]uncertain significance125135742551357425Humanname
156116364CV2349375single nucleotide variantNM_007210.4(GALNT6):c.1294G>A (p.Ala432Thr)not specified [RCV004199307]uncertain significance125135920651359206Humanname
156211096CV2378250single nucleotide variantNM_007210.4(GALNT6):c.1286T>C (p.Val429Ala)not specified [RCV004226285]uncertain significance125135921451359214Humanname
155953849CV2379092single nucleotide variantNM_007210.4(GALNT6):c.1594G>A (p.Gly532Ser)not specified [RCV004235894]uncertain significance125135735751357357Humanname
156222816CV2394738single nucleotide variantNM_007210.4(GALNT6):c.1850A>C (p.Gln617Pro)not specified [RCV004234414]uncertain significance125135439851354398Humanname
156226325CV2401126single nucleotide variantNM_007210.4(GALNT6):c.1166G>A (p.Arg389Gln)not specified [RCV004245691]uncertain significance125136072251360722Humanname
329354403CV2448112single nucleotide variantNM_007210.4(GALNT6):c.1848T>G (p.His616Gln)not specified [RCV004263333]uncertain significance125135440051354400Humanname
329370744CV2461847single nucleotide variantNM_007210.4(GALNT6):c.1022G>C (p.Arg341Thr)not specified [RCV004271762]uncertain significance125136414851364148Humanname
401781295CV2681956single nucleotide variantNM_007210.4(GALNT6):c.1277G>A (p.Arg426His)not specified [RCV004296940]uncertain significance125135922351359223Humanname
401874679CV2759316single nucleotide variantNM_007210.4(GALNT6):c.1228C>T (p.Arg410Trp)not specified [RCV004335900]uncertain significance125135927251359272Humanname
401886303CV2771161single nucleotide variantNM_007210.4(GALNT6):c.1341T>A (p.Asn447Lys)not specified [RCV004346156]uncertain significance125135915951359159Humanname
401879601CV2792037single nucleotide variantNM_007210.4(GALNT6):c.1266T>G (p.Ser422Arg)not specified [RCV004359438]uncertain significance125135923451359234Humanname
405750073CV3254523single nucleotide variantNM_007210.4(GALNT6):c.1241C>A (p.Pro414His)not specified [RCV004392603]uncertain significance125135925951359259Humanname
405750082CV3254524single nucleotide variantNM_007210.4(GALNT6):c.1372T>G (p.Ser458Ala)not specified [RCV004392604]uncertain significance125135825851358258Humanname
405750089CV3254525single nucleotide variantNM_007210.4(GALNT6):c.1388C>T (p.Ser463Leu)not specified [RCV004392605]uncertain significance125135824251358242Humanname
405750096CV3254526single nucleotide variantNM_007210.4(GALNT6):c.1549C>T (p.Arg517Cys)not specified [RCV004392606]uncertain significance125135740251357402Humanname
407503557CV3436318single nucleotide variantNM_007210.4(GALNT6):c.1735G>A (p.Glu579Lys)not specified [RCV004623791]uncertain significance125135582651355826Humanname
407503574CV3436323single nucleotide variantNM_007210.4(GALNT6):c.1585G>A (p.Gly529Ser)not specified [RCV004623796]uncertain significance125135736651357366Humanname
597779965CV3680727single nucleotide variantNM_007210.4(GALNT6):c.1864G>A (p.Val622Ile)not specified [RCV004930509]likely benign125135438451354384Humanname
597779974CV3680730single nucleotide variantNM_007210.4(GALNT6):c.1292T>C (p.Leu431Pro)not specified [RCV004930511]uncertain significance125135920851359208Humanname
597754076CV3680731single nucleotide variantNM_007210.4(GALNT6):c.1694G>A (p.Ser565Asn)not specified [RCV004924287]uncertain significance125135586751355867Humanname
597779988CV3680735single nucleotide variantNM_007210.4(GALNT6):c.1007C>T (p.Pro336Leu)not specified [RCV004930514]uncertain significance125136416351364163Humanname
597779992CV3680736single nucleotide variantNM_007210.4(GALNT6):c.1493A>G (p.Tyr498Cys)not specified [RCV004930515]uncertain significance125135813751358137Humanname
598203322CV3973934single nucleotide variantNM_007210.4(GALNT6):c.1378G>A (p.Gly460Ser)not specified [RCV005337239]uncertain significance125135825251358252Humanname
598203348CV3973938single nucleotide variantNM_007210.4(GALNT6):c.1758T>A (p.Asp586Glu)not specified [RCV005337243]uncertain significance125135449051354490Humanname
598203353CV3973939single nucleotide variantNM_007210.4(GALNT6):c.1640A>G (p.Asn547Ser)not specified [RCV005337244]uncertain significance125135592151355921Humanname
15168943CV702350single nucleotide variantNM_007210.4(GALNT6):c.1267G>A (p.Val423Ile)not provided [RCV000949361]benign125135923351359233Humanname